Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 4-Methylpiperidine | HCID 69381 | — |
| Reactant | Fumaric Acid | HCID 444972 | — |
| Reactant | HCID 15380030 | HCID 15380030 | — |
| Catalyst | Cuprous chloride | HCID 62652 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 131719460 | HCID 131719460 | — |
Reaction Steps
A mixture of 1,2-dihydro-7-(2-propynyl)-benzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepin-6-one (4.45 gm, 16.2 mmole), paraformaldehyde (3.6 gm), 4-methylpiperidine (1.93 gm, 1.2 eq) and copper(I) chloride (300 mg), in dioxane (75 ml) was stirred for 16 hours at room temperature. After the reaction was complete, the mixture was diluted with dichloromethane (DCM, 300 ml). The insolubles were filtered off through a pad of celite. The solution was concentrated on a rotary evaporator to an oil (48 gm). The desired product was purified by flash chromatography over a silica gel column (100 gm, SiO2, eluted with 1% CH3OH:1% diethylamine:98% DCM, 1.5 l). The material obtained as a yellow syrup was dissolved in ether (50 ml) and filtered once. The ethereal solution was added to a solution of fumaric acid (1.9 gm, 1.0 eq) in ether (30 ml) with fast stirring. The salt crashed out as a thick gum. This mixture was diluted with ether (300 ml) and stirred for i hour, while the gum turned slowly to a solid. The solid was collected and recrystallized once from hot ethanol to afford yellow crystals: 3.9 gm, m.p. 157°-158° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05536717 |
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| Source dataset | uspto-grants-1996_07 |
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| ORD ID | ord-d050ae3f4ea3459ca1e09b970bd40b72 |
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| Source note | uspto-grants-1996_07 |
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